2,3,6-Trifluorobenzyl bromide

98%

Reagent Code: #115160
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CAS Number 151412-02-1

science Other reagents with same CAS 151412-02-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.01 g/mol
Formula F₃C₆H₂CH₂Br
badge Registry Numbers
MDL Number MFCD00061208
thermostat Physical Properties
Melting Point 114°C (dec.)
Boiling Point 114 °C(lit.)
inventory_2 Storage & Handling
Density 1.718 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is valuable for introducing the 2,3,6-trifluorobenzyl group into larger molecules, enhancing their biological activity or modifying their chemical properties. Its reactivity makes it suitable for cross-coupling reactions and nucleophilic substitutions, enabling the creation of complex compounds. In medicinal chemistry, it is often employed to develop drug candidates with improved potency or selectivity. Additionally, it finds application in the synthesis of advanced materials and specialty chemicals, where its fluorine atoms contribute to unique properties such as stability and resistance to degradation.

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Test Parameter Specification
Purity (HPLC) 98-100
Refractive Index (N20/D) 1.507-1.509
Appearance Colorless to light yellow liquid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,107.00
inventory 5g
10-20 days ฿4,068.00

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2,3,6-Trifluorobenzyl bromide
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Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is valuable for introducing the 2,3,6-trifluorobenzyl group into larger molecules, enhancing their biological activity or modifying their chemical properties. Its reactivity makes it suitable for cross-coupling reactions and nucleophilic substitutions, enabling the creation of complex compounds. In medicinal chemistry, it is often employed to develop drug candidates with improve

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is valuable for introducing the 2,3,6-trifluorobenzyl group into larger molecules, enhancing their biological activity or modifying their chemical properties. Its reactivity makes it suitable for cross-coupling reactions and nucleophilic substitutions, enabling the creation of complex compounds. In medicinal chemistry, it is often employed to develop drug candidates with improved potency or selectivity. Additionally, it finds application in the synthesis of advanced materials and specialty chemicals, where its fluorine atoms contribute to unique properties such as stability and resistance to degradation.

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